Tag | Content |
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EnhancerAtlas ID | HS037-18343 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr19:50248650-50249720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP1 | MA0079.4 | chr19:50248993-50249008 | TAAGCCCCGCCCACC | + | 7.09 | SP2 | MA0516.2 | chr19:50248992-50249009 | CTAAGCCCCGCCCACCT | + | 9.12 | SP4 | MA0685.1 | chr19:50248993-50249010 | TAAGCCCCGCCCACCTC | + | 7.17 | Zfx | MA0146.2 | chr19:50249200-50249214 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I049746 | chr19 | 50249300 | 50250044 |
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Enhancer Sequence | CTCCTGGAGG GGCAGAGGAG GGGAATGGGT AGGGGCTAGG CTTCAACAGG TCCCCACCTA 60 CCCCCACGAG ATAGGTGGGA CAGGACTCAC CTATCTCGCC CCACTGAGAC CATGCCCGTG 120 GCTCCAGACC CACCCAGGTC ACCAAATTTT ATTGCACCCT CCATTTGGTG AAATTTGGTC 180 GTGTCCTCCA GAGCCCCGCC TTTATCCCCT TCCTTTATTG GCTATCTTGG CCCTTTCCTG 240 GTCAGGTCCC CAACCTCTAC CTGGGCTCCT CCAGACACTG GCCCCCCAAG GCACTGCCCA 300 CCCTACTCTG CCCCACGTGG TGCCTCCAGG ACCACTCCTC TCCTAAGCCC CGCCCACCTC 360 AGTTTCACCA GGCCTGGACC TGCCTCCCAG CAGCCCAGAA CTAAAAAGTT CCTTATTCTG 420 TCCCTCCCTT GCTCAGGTCA CTGCCTTCGG GGCACTCCCT CCTCTGCTCT TGGAGACCCC 480 AGCCTTGTCG CCTTCCGGTT AAGATCTAGG CCGGGCGCGG TGGCTCACGC CTGTAATCCT 540 AGCACTTTGG GAGGCCGAGG CGGGCGGATC ACGAGGCCAG GAGATCGAGG CCATCCTGGC 600 TAACACGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAA ATAGCCAGGC GTGGTGGCGG 660 GCGCCTGTAG TCCCAGCTAT TGGGGAGGCT GAAGCAGGAG AATGGCGTGA ACCCGGGAGG 720 CGGAGCTTGC AGTGAGCCAA GACGGCGCCA CTGCACTCCA GCCTGGGCGA CAAGCGAGAC 780 TCCGCCTCAA AAAAAACAAA ACAAAACAAA AAACGATCTT TGAGGAACCT CCCCTGTGTC 840 CCCGCCCACC GCAGCTCCTG GAGACTCCTC CCGTGTCTCT ACCCACCTTC GTTCCTCGAG 900 GCTCCTCCCA TGTTCCCGCC CACCTCAGGT CCCCGAGGCT CCACCCATGT CACCGCCCAC 960 CTCAGCTACT TGAGAACCCC CGTCCCTTGG GTCCCGCCCA CCGCATCTCC TCGAGGCTCC 1020 ACCCCTGAGT CCCCGCCGAT CTCGTTTTCG AGGCTCCGCC CCTAGGTCCC 1070
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